ZA200006385B - Antigenic complex comprising immunostimulatory peptide, CD4, and chemokine receptor domain for HIV treatment and immune disorders. - Google Patents
Antigenic complex comprising immunostimulatory peptide, CD4, and chemokine receptor domain for HIV treatment and immune disorders. Download PDFInfo
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- ZA200006385B ZA200006385B ZA200006385A ZA200006385A ZA200006385B ZA 200006385 B ZA200006385 B ZA 200006385B ZA 200006385 A ZA200006385 A ZA 200006385A ZA 200006385 A ZA200006385 A ZA 200006385A ZA 200006385 B ZA200006385 B ZA 200006385B
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- South Africa
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- peptide
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
- C07K14/70503—Immunoglobulin superfamily
- C07K14/70514—CD4
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Zoology (AREA)
- Biophysics (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Genetics & Genomics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Biochemistry (AREA)
- Gastroenterology & Hepatology (AREA)
- Cell Biology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US09/100,409 US6090388A (en) | 1998-06-20 | 1998-06-20 | Peptide composition for prevention and treatment of HIV infection and immune disorders |
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ZA200006385B true ZA200006385B (en) | 2001-10-11 |
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ZA200006385A ZA200006385B (en) | 1998-06-20 | 2000-11-07 | Antigenic complex comprising immunostimulatory peptide, CD4, and chemokine receptor domain for HIV treatment and immune disorders. |
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US (1) | US6090388A (zh) |
EP (1) | EP1098910B1 (zh) |
JP (1) | JP4216473B2 (zh) |
CN (1) | CN1207306C (zh) |
AT (1) | ATE447585T1 (zh) |
AU (1) | AU766955B2 (zh) |
BR (1) | BRPI9912175B1 (zh) |
CA (1) | CA2330235C (zh) |
DE (1) | DE69941625D1 (zh) |
DK (1) | DK1098910T3 (zh) |
ES (1) | ES2336393T3 (zh) |
HK (1) | HK1036805A1 (zh) |
TW (1) | TWI227242B (zh) |
WO (1) | WO1999067294A1 (zh) |
ZA (1) | ZA200006385B (zh) |
Families Citing this family (38)
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US6417324B1 (en) * | 2000-04-21 | 2002-07-09 | Tripep Ab | Synthetic peptides that bind to the hepatitis B virus core and e antigens |
US6660842B1 (en) | 1994-04-28 | 2003-12-09 | Tripep Ab | Ligand/receptor specificity exchangers that redirect antibodies to receptors on a pathogen |
US6040137A (en) * | 1995-04-27 | 2000-03-21 | Tripep Ab | Antigen/antibody specification exchanger |
US6933366B2 (en) * | 1996-12-27 | 2005-08-23 | Tripep Ab | Specificity exchangers that redirect antibodies to bacterial adhesion receptors |
US20030054012A1 (en) * | 2000-05-12 | 2003-03-20 | Fitzgerald David J. | Pseudomonas exotoxin a-like chimeric immunogens for eliciting a secretory iga-mediated immune response |
CA2295971C (en) * | 1997-07-11 | 2011-02-08 | THE GOVERNMENT OF THE UNITED STATES, represented by THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES | Pseudomonas exotoxin a-like chimeric immunogens |
US7314632B1 (en) * | 1997-07-11 | 2008-01-01 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Pseudomonas exotoxin A-like chimeric immunogens |
TWI229679B (en) * | 1998-06-20 | 2005-03-21 | United Biomedical Inc | Artificial T helper cell epitopes as immune stimulators for synthetic peptide immunogens |
EP1141313A2 (en) * | 1998-12-31 | 2001-10-10 | Chiron Corporation | Improved expression of hiv polypeptides and production of virus-like particles |
AU2487300A (en) | 1998-12-31 | 2000-07-31 | Chiron Corporation | Polynucleotides encoding antigenic hiv type c polypeptides, polypeptides and uses thereof |
US7935805B1 (en) * | 1998-12-31 | 2011-05-03 | Novartis Vaccines & Diagnostics, Inc | Polynucleotides encoding antigenic HIV Type C polypeptides, polypeptides and uses thereof |
WO2000039303A2 (en) | 1998-12-31 | 2000-07-06 | Chiron Corporation | Modified hiv env polypeptides |
WO2002004499A1 (en) * | 2000-07-12 | 2002-01-17 | Gryphon Therapeutics, Inc. | Chemokine receptor modulators, production and use |
US7118737B2 (en) | 2000-09-08 | 2006-10-10 | Amylin Pharmaceuticals, Inc. | Polymer-modified synthetic proteins |
AU2001273388B2 (en) * | 2000-09-08 | 2005-01-13 | Gryphon Therapeutics, Inc. | "Pseudo"-native chemical ligation |
CA2438515A1 (en) * | 2001-02-15 | 2002-08-22 | The Government Of The United States Of America | Methods and compositions for inhibiting hiv-coreceptor interactions |
US20040077835A1 (en) * | 2001-07-12 | 2004-04-22 | Robin Offord | Chemokine receptor modulators, production and use |
WO2003020876A2 (en) * | 2001-08-31 | 2003-03-13 | Chiron Corporation | Polynucleotides encoding antigenic hiv type b polypeptides, polypeptides and uses thereof |
US8088388B2 (en) | 2002-02-14 | 2012-01-03 | United Biomedical, Inc. | Stabilized synthetic immunogen delivery system |
US20060147477A1 (en) * | 2002-06-11 | 2006-07-06 | Glaxo Group Limited | Immunogenic compositions |
AU2003251053B2 (en) * | 2002-08-13 | 2009-11-19 | Haptogen Ltd | Methods for the treatment of an infectious bacterial disease with an anti-lactone or lactone derived signal molecules antibody |
EP2230249A3 (en) * | 2003-02-06 | 2010-12-22 | ChronTech Pharma AB | Antigen/antibody or ligand/receptor glycosylated specificity exchangers |
US7335359B2 (en) * | 2003-02-06 | 2008-02-26 | Tripep Ab | Glycosylated specificity exchangers |
GB0407008D0 (en) * | 2004-03-27 | 2004-04-28 | Haptogen Ltd | Methods for inducing rapid cell death (autolysis) in infectious bacteria |
GB0410958D0 (en) * | 2004-05-15 | 2004-06-16 | Haptogen Ltd | Methods for reducing biofilm formation in infectious bacteria |
US9340601B2 (en) * | 2007-03-01 | 2016-05-17 | The Board Of Trustees Of The Leland Stanford Junior University | Splice variants of the EGF receptor |
US20090092631A1 (en) * | 2007-03-26 | 2009-04-09 | Tripep Ab | Glycosylated specificity exchangers that induce an antibody dependent cellular cytotoxicity (adcc) response |
US8501907B2 (en) | 2007-08-10 | 2013-08-06 | Janssen Biotech, Inc. | Immunoglobulin cleavage fragments as disease indicators and compositions for detecting and binding such |
ITPA20080007A1 (it) * | 2008-03-19 | 2009-09-20 | Angela Bonura | Fattore anti - lps da parietaria judaica e suoi metodi di utilizzo. |
TW201029663A (en) | 2008-11-12 | 2010-08-16 | Theraclone Sciences Inc | Human M2e peptide immunogens |
US20110305670A1 (en) * | 2010-06-10 | 2011-12-15 | President And Fellows Of Harvard College | Nucleic acid encoding fusion polypeptides that prevent or inhibit hiv infection |
RU2535033C2 (ru) * | 2010-08-06 | 2014-12-10 | Олег Ильич Эпштейн | Лекарственное средство и способ профилактики инфицирования вич, профилактики и лечения заболеваний, вызываемых вич или ассоциированных с вич, в том числе спида |
MX2013005646A (es) * | 2010-11-19 | 2013-08-01 | Janssen Biotech Inc | Composiciones de vacuna de fragmentos de clivaje de la inmunoglobulina. |
CN102380094B (zh) * | 2011-10-11 | 2013-08-07 | 中国科学院微生物研究所 | 特异多肽在制备狂犬病疫苗中的应用 |
US11180555B2 (en) | 2014-09-16 | 2021-11-23 | Ubi Us Holdings, Llc. | Antibodies directed against CD4 for the treatment and functional cure of HIV |
EP3497133A4 (en) | 2016-08-13 | 2020-03-25 | UBI IP Holdings | TREATMENT AND DELAYED VIROLOGICAL REMISSION OF HIV INFECTIONS BY ANTIBODIES AGAINST CD4 IN HAIR-STABILIZED PATIENTS |
CN108640977A (zh) * | 2018-06-18 | 2018-10-12 | 上海大学 | 特异性结合HIV上包膜糖蛋白gp120的多肽及其应用 |
CN113318225B (zh) * | 2020-02-28 | 2024-01-19 | 无锡派列博生物医药科技有限公司 | 肿瘤免疫增强剂及其制法和应用 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0768273B2 (ja) * | 1988-12-02 | 1995-07-26 | カルピス食品工業株式会社 | 抗hivペプチド |
US5106726A (en) * | 1990-02-16 | 1992-04-21 | United Biomedical, Inc. | Synthetic peptides specific for the detection of antibodies to HCV |
JP3795914B2 (ja) * | 1993-04-27 | 2006-07-12 | ユナイテッド・バイオメディカル・インコーポレイテッド | ワクチン用免疫原性lhrhペプチド構築体および合成普遍免疫刺激器 |
US5759551A (en) * | 1993-04-27 | 1998-06-02 | United Biomedical, Inc. | Immunogenic LHRH peptide constructs and synthetic universal immune stimulators for vaccines |
EP0725838A4 (en) * | 1993-10-26 | 1997-02-26 | United Biomedical Inc | STRUCTURED SYNTHETIC ANTIGAN BANKS AS DIAGNOSTICS, VACCINE AND THERAPEUTIC AGENTS |
CN1146772A (zh) * | 1994-03-28 | 1997-04-02 | 美国联合生物医学公司 | 用于治疗过敏反应的合成肽免疫原 |
CA2256306C (en) * | 1996-06-03 | 2011-03-29 | United Biomedical, Inc. | Antibodies against a complex of cd4 and a chemokine receptor domain, and their use against hiv infections |
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1998
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- 1999-06-21 DE DE69941625T patent/DE69941625D1/de not_active Expired - Lifetime
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JP4216473B2 (ja) | 2009-01-28 |
JP2002518523A (ja) | 2002-06-25 |
BRPI9912175A (pt) | 2001-04-10 |
AU4704899A (en) | 2000-01-10 |
ATE447585T1 (de) | 2009-11-15 |
ES2336393T3 (es) | 2010-04-12 |
EP1098910B1 (en) | 2009-11-04 |
DE69941625D1 (de) | 2009-12-17 |
US6090388A (en) | 2000-07-18 |
EP1098910A4 (en) | 2005-02-02 |
EP1098910A1 (en) | 2001-05-16 |
CN1303394A (zh) | 2001-07-11 |
TWI227242B (en) | 2005-02-01 |
BRPI9912175B1 (pt) | 2019-08-27 |
CA2330235C (en) | 2008-08-12 |
HK1036805A1 (en) | 2002-01-18 |
CA2330235A1 (en) | 1999-12-29 |
CN1207306C (zh) | 2005-06-22 |
WO1999067294A1 (en) | 1999-12-29 |
AU766955B2 (en) | 2003-10-30 |
DK1098910T3 (da) | 2010-02-01 |
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